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1375748-59-6

C61H87F3O13 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1375748-59-6 Structure

  • Basic information

    1. Product Name: C61H87F3O13
    2. Synonyms:
    3. CAS NO:1375748-59-6
    4. Molecular Formula:
    5. Molecular Weight: 1085.35
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1375748-59-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: C61H87F3O13(CAS DataBase Reference)
    10. NIST Chemistry Reference: C61H87F3O13(1375748-59-6)
    11. EPA Substance Registry System: C61H87F3O13(1375748-59-6)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1375748-59-6(Hazardous Substances Data)

1375748-59-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1375748-59-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,5,7,4 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1375748-59:
(9*1)+(8*3)+(7*7)+(6*5)+(5*7)+(4*4)+(3*8)+(2*5)+(1*9)=206
206 % 10 = 6
So 1375748-59-6 is a valid CAS Registry Number.

1375748-59-6Downstream Products

1375748-59-6Relevant articles and documents

Bahamaolides A and B, antifungal polyene polyol macrolides from the marine actinomycete streptomyces sp.

Kim, Dong-Gyu,Moon, Kyuho,Kim, Seong-Hwan,Park, Seon-Hui,Park, Sunghyouk,Lee, Sang Kook,Oh, Ki-Bong,Shin, Jongheon,Oh, Dong-Chan

, p. 959 - 967 (2012)

Bahamaolides A and B (1 and 2), two new 36-membered macrocyclic lactones, were isolated from the culture of the marine actinomycete Streptomyces sp. derived from a sediment sample collected at North Cat Cay in the Bahamas. The planar structures of 1 and 2, bearing a hexaenone and nine consecutive skipped hydroxy groups, were determined by 1D and 2D NMR, mass, IR, and UV spectra. The absolute configurations of the bahamaolides were established by combined multistep chemical reactions and spectroscopic analysis. Bahamaolide A displayed significant inhibitory activity against Candida albicans isocitrate lyase and antifungal activity against various pathogenic fungi.

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